Registration number (WIID)Project No.TitleStatus
9471LVS EN 30993-1:1994Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992)Atcelts
9500EN ISO 10993-18:2005Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)Atcelts
32001EN ISO 10993-15:2009Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)Atcelts
9471EN 30993-1:1994Biological evaluation of medical devices - Part 1: Guidance on selection of tests (ISO 10993-1:1992 + Technical Corrigendum 1:1992)Atcelts
9501LVS EN ISO 10993-10:2003Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivityAtcelts
9499LVS EN ISO 10993-17:2003Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substancesAtcelts
9472LVS EN 30993-5:1994Biological evaluation of medical devices - Part 5: Tests for cytotoxicity - in vitro methods (ISO 10993-5:1992)Atcelts
31982LVS EN ISO 10993-10:2009Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity (ISO 10993-10:2002, including Amd 1:2006)Atcelts
31999LVS EN ISO 10993-13:2009Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:1998)Atcelts
32006LVS EN ISO 10993-6:2009Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)Atcelts
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